LymeNet Home LymeNet Home Page LymeNet Flash Discussion LymeNet Support Group Database LymeNet Literature Library LymeNet Legal Resources LymeNet Medical & Scientific Abstract Database LymeNet Newsletter Home Page LymeNet Recommended Books LymeNet Tick Pictures Search The LymeNet Site LymeNet Links LymeNet Frequently Asked Questions About The Lyme Disease Network LymeNet Menu

LymeNet on Facebook

LymeNet on Twitter




The Lyme Disease Network receives a commission from Amazon.com for each purchase originating from this site.

When purchasing from Amazon.com, please
click here first.

Thank you.

LymeNet Flash Discussion
Dedicated to the Bachmann Family

LymeNet needs your help:
LymeNet 2020 fund drive


The Lyme Disease Network is a non-profit organization funded by individual donations.

LymeNet Flash Post New Topic  New Poll  Post A Reply
my profile | directory login | register | search | faq | forum home

  next oldest topic   next newest topic
» LymeNet Flash » Questions and Discussion » Medical Questions » bottom of feet pain

 - UBBFriend: Email this page to someone!    
Author Topic: bottom of feet pain
Marcie
LymeNet Contributor
Member # 10070

Icon 1 posted      Profile for Marcie     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hi,
Does anyone know if bottom of feet pain/soreness would be a co-infection symptom, Lyme, or both? My feet have been very sore.
marcie

Posts: 323 | From Michigan | Registered: Sep 2006  |  IP: Logged | Report this post to a Moderator
kelmo
Frequent Contributor (1K+ posts)
Member # 8797

Icon 1 posted      Profile for kelmo     Send New Private Message       Edit/Delete Post   Reply With Quote 
My daughter has it with bart. I don't know if it's a common symptom.
Posts: 2903 | From AZ | Registered: Feb 2006  |  IP: Logged | Report this post to a Moderator
GiGi
Frequent Contributor (5K+ posts)
Member # 259

Icon 1 posted      Profile for GiGi         Edit/Delete Post   Reply With Quote 
As another choide: It's always been a metal symptom. Gravity.

Take care.

Posts: 9834 | From Washington State | Registered: Oct 2000  |  IP: Logged | Report this post to a Moderator
Aniek
Frequent Contributor (1K+ posts)
Member # 5374

Icon 1 posted      Profile for Aniek     Send New Private Message       Edit/Delete Post   Reply With Quote 
I've always heard it was a bart symptom. Mine was worst on drugs that reach bart - Biaxin and Levaquin.

--------------------
"When there is pain, there are no words." - Toni Morrison

Posts: 4711 | From Washington, DC | Registered: Mar 2004  |  IP: Logged | Report this post to a Moderator
SForsgren
Frequent Contributor (1K+ posts)
Member # 7686

Icon 1 posted      Profile for SForsgren         Edit/Delete Post   Reply With Quote 
Bartonella. I agree.

--------------------
Be well,
Scott

Posts: 4617 | From San Jose, CA | Registered: Jul 2005  |  IP: Logged | Report this post to a Moderator
Jill E.
Frequent Contributor (1K+ posts)
Member # 9121

Icon 1 posted      Profile for Jill E.     Send New Private Message       Edit/Delete Post   Reply With Quote 
That symptom came on during Bartonella treatment and has remained because I had to go off Bartonella treatment early. Never had the symptom before that. So for me, it's Bartonella.

Jill

--------------------
If laughter is the best medicine, why hasn't stand-up comedy cured me?

Posts: 1773 | From San Diego | Registered: Apr 2006  |  IP: Logged | Report this post to a Moderator
lymeout
LymeNet Contributor
Member # 8045

Icon 1 posted      Profile for lymeout     Send New Private Message       Edit/Delete Post   Reply With Quote 
Does Bicillin LA work for bartonella? My daughter just started injections and is herxing madly, but one symptom that she rarely complained of previously but is now particularly strong, is sore bottoms of feet, especially in the morning.
We were suspecting bart back in the winter, but test came back negative.

Posts: 422 | From Herndon, Virginia | Registered: Oct 2005  |  IP: Logged | Report this post to a Moderator
5dana8
Frequent Contributor (1K+ posts)
Member # 7935

Icon 1 posted      Profile for 5dana8   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
Bart [Frown]

--------------------
5dana8

Posts: 4432 | From some where over the rainbow | Registered: Sep 2005  |  IP: Logged | Report this post to a Moderator
hatsnscarfs
LymeNet Contributor
Member # 6562

Icon 1 posted      Profile for hatsnscarfs     Send New Private Message       Edit/Delete Post   Reply With Quote 
Sore soles for me means Lyme, herxing and toxins. I get relief by using podi patches every night www.akgnaturals.com. You can find lots more info about these detox patches by doing a search on LymeNet.

Soaking in Epsom salts (2 cups/tub) also makes my feet feel better.
hats

Posts: 956 | From MA | Registered: Nov 2004  |  IP: Logged | Report this post to a Moderator
umbies are great
Junior Member
Member # 10217

Icon 1 posted      Profile for umbies are great   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
My LLMD said it was due to periferal nerve damage from lyme dz. Lyme can affect your CNS (BRAIN &SPINAL CORD). This includes the radicular nerve which is the primary nerve for the bottom of the foot. My tx is Lyrica; 75mg 2xs a day. It takes care of the pain. It is fairly new. It is one step above neurotin. Diabetics often suffer from the same type of pain and take neurotin for it. Hope this info helps.
Posts: 5 | From Brandon, MS | Registered: Sep 2006  |  IP: Logged | Report this post to a Moderator
Jill E.
Frequent Contributor (1K+ posts)
Member # 9121

Icon 1 posted      Profile for Jill E.     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hi again,

I posted earlier that my sore soles came on during Bart treatment. However, I will second the post that mentions Lyme die-off and the use of Podi Patches.

Also, the famous Dr. B., on a DVD of one of his speeches, mentioned sore soles as being consistent with Bart.

By the way, my Bart test did not turn positive until after I started Bart medication - but I was symptomatic before that.

I've been on Bicillin for months. My LLMD was also considering that the foot pain could be due to Lyme die-off in areas of the body that don't get a lot of circulation/oxygen. I'm not much of a herxer, even on Bicillin, but the Bicillin could certainly be adding to it. Bicillin is for Lyme, not Bartonella.

I've recently started using the Podi Patches hoping it would help my foot pain/Achilles tendon pain. I think they do help a bit. I haven't been doing them long enough to really know for sure.

I do have burning peripheral neuropathy throughout my entire body from Lyme or coinfections, but the sore soles came on years after the onset of the neuropathy.

Take care,
Jill

--------------------
If laughter is the best medicine, why hasn't stand-up comedy cured me?

Posts: 1773 | From San Diego | Registered: Apr 2006  |  IP: Logged | Report this post to a Moderator
kelmo
Frequent Contributor (1K+ posts)
Member # 8797

Icon 1 posted      Profile for kelmo     Send New Private Message       Edit/Delete Post   Reply With Quote 
My daughter and I were taking a walk tonight...can you believe it? Taking a walk!!

A year ago she would not have been able to do it.

She said the soles of her feet don't hurt any more in the morning. Her hands still hurt, but the feet are doing fine.

She has tested positive for Bart only. So, Zith and Rifampin have helped that symptom. There are still many more to go.

Kelly

Posts: 2903 | From AZ | Registered: Feb 2006  |  IP: Logged | Report this post to a Moderator
seibertneurolyme
Frequent Contributor (5K+ posts)
Member # 6416

Icon 1 posted      Profile for seibertneurolyme     Send New Private Message       Edit/Delete Post   Reply With Quote 
I don't have Lyme -- hubby does. For me, sore soles of the feet in the a.m. were a sign of high blood pressure. I would limp into the bathroom in the mornings and then would have no more problems during the day when my circulation was better.

Bea Seibert

Posts: 7306 | From Martinsville,VA,USA | Registered: Oct 2004  |  IP: Logged | Report this post to a Moderator
sadie420
LymeNet Contributor
Member # 9294

Icon 1 posted      Profile for sadie420     Send New Private Message       Edit/Delete Post   Reply With Quote 
I have had Lyme for 14 years and only this year developed that symptom - pain on the sole of one foot, especially in the morning, as others are reporting. I am glad to learn it is yet another symptom of Lyme as I was considering seeing a podiatrist.

Strange critters, aren't they!

Sadie

Posts: 115 | From new york | Registered: May 2006  |  IP: Logged | Report this post to a Moderator
Marcie
LymeNet Contributor
Member # 10070

Icon 1 posted      Profile for Marcie     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hi,
Thanks for the many suggestions. I am hoping it is a toxin die off of lyme and not Bart, but when I finally see the LLMD I will ask. I live in Michigan and there are only a few LLMD here so it's taking a while to get in. For now, I did find a doctor who put me on 400mg of doxy a day. Before I started the doxy I was having some nerve problems like burning sensations in legs. I am wondering if the foot pain has to do with that?
Marcie

Posts: 323 | From Michigan | Registered: Sep 2006  |  IP: Logged | Report this post to a Moderator
5dana8
Frequent Contributor (1K+ posts)
Member # 7935

Icon 1 posted      Profile for 5dana8   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
Here's a previous discussion on foot pain:

http://flash.lymenet.org/scripts/ultimatebb.cgi?ubb=get_topic;f=1;t=045097

--------------------
5dana8

Posts: 4432 | From some where over the rainbow | Registered: Sep 2005  |  IP: Logged | Report this post to a Moderator
cindy_leigh
LymeNet Contributor
Member # 3514

Icon 1 posted      Profile for cindy_leigh     Send New Private Message       Edit/Delete Post   Reply With Quote 
I ended up with plantar fasciitis with lyme
also a peripheral neuropathy that waxes and wanes.

Posts: 688 | From CT | Registered: Jan 2003  |  IP: Logged | Report this post to a Moderator
healthywealthywise
LymeNet Contributor
Member # 8595

Icon 1 posted      Profile for healthywealthywise     Send New Private Message       Edit/Delete Post   Reply With Quote 
I hobbled so badly with the foot pain in my heels. Abx didn't help it....neither did patches.

The only relief I got was to have my podiatrist inject my plantar tendons with cortisone.

I know.....cortisone is a no-no for lymies, but it is and continues to be the only thing that takes the pain away.

I only do it every 6 months or so when it comes back again.

Posts: 867 | From PA | Registered: Jan 2006  |  IP: Logged | Report this post to a Moderator
Laurie
LymeNet Contributor
Member # 159

Icon 1 posted      Profile for Laurie   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
I have had bouts of horrendous bottom-of-feet pain, lasting weeks, but ONLY first thing in the morning (or sometimes when getting out of bed during the night). This is plantar fasciitis. It does seem to be a Lyme or co-infection symptom. What helped me more than anything is a pair of $15 gel heel-cups rx'd by my family doctor.
Posts: 459 | From Connecticut - just across the river from the Lymes (Old Lyme, Hadlyme, East Lyme, South Lyme & Lyme) | Registered: Oct 2000  |  IP: Logged | Report this post to a Moderator
Dean L. Harris
Member
Member # 9969

Icon 1 posted      Profile for Dean L. Harris     Send New Private Message       Edit/Delete Post   Reply With Quote 
Have had foot and heel pain for years and not knowing of/aware of Lyme used the heel cups (they are called Tuli Heel Cup and are available in the foot section of any drug store) and also had foot surgery for which the surgeon fitted me with a hard plastic support for the metatarsals which had a cup shape for the heel. Now I find that any shoe (Birke whatever) that shapes to the heel seems to eliminate the pain after the first step out of bed to get into the shoe/slipper/etc.
Posts: 13 | From Fort Wayne, IN | Registered: Aug 2006  |  IP: Logged | Report this post to a Moderator
DeniseS
LymeNet Contributor
Member # 7276

Icon 1 posted      Profile for DeniseS     Send New Private Message       Edit/Delete Post   Reply With Quote 
I have to reiterate the Bart idea.

After 1.5 years of Lyme and Babs tx I was feeling a lot better but had lingering sx. I read SF's summary of what Dr. B said at a conference about Bart and sore soles and the lightbulb went off. I hadn't even thought to mention this sx to my docs before. I requested Levaquin and have been herxing increasingly for 10 weeks! All three of my LLMDs think that this is it. The Bart herx is exactly the sx that weren't going away.

My Bart test still remains negative.

Also, I had been doing PodiPatches the entire length of my tx.

The herx is the worst of my whole tx but I know it's going to make a big diff in how I feel.

My heart goes out to you and your daughter,
D

Posts: 261 | From San Mateo, CA | Registered: May 2005  |  IP: Logged | Report this post to a Moderator
hanoverw/lyme
Member
Member # 10215

Icon 1 posted      Profile for hanoverw/lyme     Send New Private Message       Edit/Delete Post   Reply With Quote 
quote:
Originally posted by Marcie:
Hi,
Does anyone know if bottom of feet pain/soreness would be a co-infection symptom, Lyme, or both? My feet have been very sore.
marcie


Posts: 46 | From hanover, pa | Registered: Sep 2006  |  IP: Logged | Report this post to a Moderator
hanoverw/lyme
Member
Member # 10215

Icon 1 posted      Profile for hanoverw/lyme     Send New Private Message       Edit/Delete Post   Reply With Quote 
my foot pain came about just resently. i tested negitive for co-infections. my antibotics were stopped to soon. within 7 weeks off of them i felt worse than when first diagnosed, intense foot pain was then a new problem.
Posts: 46 | From hanover, pa | Registered: Sep 2006  |  IP: Logged | Report this post to a Moderator
BlueRoo
Junior Member
Member # 10233

Icon 5 posted      Profile for BlueRoo     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hi. I'm new to this site and so glad I've discovered it. I have been sick for 7 yrs. and was recently diagnosed by Dr. C in MO with Lyme's. I am really curious about this 'foot pain' issue, b/c I have been experiencing a lot of pain myself. My problem is that I can't walk around barefoot at all. It makes the bones in my feet/legs hurt too much. Is the pain that ya'll are refering to more muscular or bone-related? Also, what is Bartonella?
Posts: 6 | From Virginia | Registered: Sep 2006  |  IP: Logged | Report this post to a Moderator
DeniseS
LymeNet Contributor
Member # 7276

Icon 1 posted      Profile for DeniseS     Send New Private Message       Edit/Delete Post   Reply With Quote 
Welcome BlueRoo,

Bartonella is another bacteria trasmitted by ticks aka a coinfection.

For me the pain was as if the pads under the bones in my feet were not thick enuf, were not cushioning enuf so my feet ached and felt sore in the soles and the bones.

D

Posts: 261 | From San Mateo, CA | Registered: May 2005  |  IP: Logged | Report this post to a Moderator
tabbytamer
Frequent Contributor (1K+ posts)
Member # 3159

Icon 1 posted      Profile for tabbytamer     Send New Private Message       Edit/Delete Post   Reply With Quote 
Mine was diagnosed as Plantar Faciitis (left heel/foot). But it started to be unbearable when I was on Amox/Biaxin/Plaquenil combo.

After several months it seemed to improve.

Pain returned while on a break from all abx except this time in the right heel/foot.

--------------------
Tabby

 -

California Lyme support group

Posts: 2098 | From San Diego, CA, USA | Registered: Sep 2002  |  IP: Logged | Report this post to a Moderator
   

Quick Reply
Message:

HTML is not enabled.
UBB Code� is enabled.

Instant Graemlins
   


Post New Topic  New Poll  Post A Reply Close Topic   Feature Topic   Move Topic   Delete Topic next oldest topic   next newest topic
 - Printer-friendly view of this topic
Hop To:


Contact Us | LymeNet home page | Privacy Statement

Powered by UBB.classic™ 6.7.3


The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:

The Lyme Disease Network of New Jersey
907 Pebble Creek Court, Pennington, NJ 08534 USA


| Flash Discussion | Support Groups | On-Line Library
Legal Resources | Medical Abstracts | Newsletter | Books
Pictures | Site Search | Links | Help/Questions
About LymeNet | Contact Us

© 1993-2020 The Lyme Disease Network of New Jersey, Inc.
All Rights Reserved.
Use of the LymeNet Site is subject to Terms and Conditions.